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SPRY1 deficiency in skin cells causes stem cells to move to the skin surface, leading to increased pigmentation.

Oxytocin receptors are found in skin cells near touch and pain neurons.

Caspase-1 helps hair stem cells move to heal wounded or inflamed skin.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

A wireless, battery-free system uses Wi-Fi signals to enhance wound healing and enable smart healthcare at home.

A new portable microscope can effectively monitor skin wound healing in real-time.

A new laser-based microscope can clearly image biological structures without labels.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

Gap junctions help control feather pattern formation in chickens.

PBX1 helps reduce aging and cell death in hair follicle stem cells by decreasing DNA damage, not by improving DNA repair.

A new model helps study acne and test treatments.

A gene mutation in mice causes severe skin disorder similar to a human condition.

Potassium channel openers help form elastic fibers in arteries and can treat elastin deficiency and hypertension.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

PPAR activation can improve diabetic wound healing by enhancing blood vessel function.

The OVOL1-OVOL2 axis is important for hair follicle differentiation and can help diagnose certain hair-related tumors.

Finasteride can prevent breast cancer progression by blocking progesterone's conversion to a cancer-promoting hormone.

Four transcription factors can convert mouse cells into hair cell-like cells, aiding hearing loss research and treatment.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

Prominin-1 expressing cells in the dermal papilla help regulate hair follicle size and communication but don't aid in skin repair.

A peptide known for reducing wrinkles also effectively inhibits an enzyme linked to skin inflammation and acne.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

Peripheral treatments showed some improvement in sexual dysfunction, but central symptoms remain challenging.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.